Comparator Study Evaluating Patient Experience And Preference Of FFNS vs. FPNS

NCT ID: NCT00519636

Last Updated: 2016-12-09

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE4
• Total Enrollment: 360 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2007-08-31
• Study Completion Date: 2007-11-30

Brief Summary

The purpose of this replicate study to FFU105924 is to provide data on subject preference of FFNS as compared with FPNS.

Detailed Description

A Randomized, Double-Blind, Placebo-Controlled, Active Comparator, One-Week, Cross-Over, Multicenter Study to Evaluate the Efficacy, Patient Preference and Experience of One-Daily, Intranasal Administration of 110mcg Fluticasone Furoate Nasal Spray and 200mcg Fluticasone Propionate Nasal Spray in Adult Subjects with Seasonal Allergic Rhinitis (FFU105927)

Conditions

Rhinitis, Allergic, Perennial

Keywords

experience; GW685698X; fluticasone furoate; preference; seasonal allergic rhinitis; fluticasone propionate

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: TREATMENT
• Blinding Strategy: TRIPLE

Study Groups

FFNS, FPNS

fluticasone furoate nasal spray, fluticasone propionate nasal spray

Group Type: ACTIVE_COMPARATOR

FPNS

Intervention Type: DRUG

fluticasone propionate nasal spray

FFNS

Intervention Type: DRUG

fluticasone furoate nasal spray

FPNS, FFNS

fluticasone propionate nasal spray, fluticasone furoate nasal spray

Group Type: ACTIVE_COMPARATOR

FPNS

Intervention Type: DRUG

fluticasone propionate nasal spray

FFNS

Intervention Type: DRUG

fluticasone furoate nasal spray

placebo FFNS, placebo FPNS

placebo nasal spray matching fluticasone furoate nasal spray, placebo nasal spray matching fluticasone propionate nasal spray

Group Type: PLACEBO_COMPARATOR

placebo FFNS

Intervention Type: DRUG

placebo nasal spray matching fluticasone furoate nasal spray

placebo FPNS

Intervention Type: DRUG

placebo nasal spray matching fluticasone propionate nasal spray

placebo FPNS, placebo FFNS

placebo nasal spray matching fluticasone propionate nasal spray, placebo nasal spray matching fluticasone furoate nasal spray

Group Type: PLACEBO_COMPARATOR

placebo FFNS

Intervention Type: DRUG

placebo nasal spray matching fluticasone furoate nasal spray

placebo FPNS

Intervention Type: DRUG

placebo nasal spray matching fluticasone propionate nasal spray

Interventions

FPNS

fluticasone propionate nasal spray

Intervention Type: DRUG

FFNS

fluticasone furoate nasal spray

Intervention Type: DRUG

placebo FFNS

placebo nasal spray matching fluticasone furoate nasal spray

Intervention Type: DRUG

placebo FPNS

placebo nasal spray matching fluticasone propionate nasal spray

Intervention Type: DRUG

Other Intervention Names

fluticasone propionate; fluticasone furoate

Eligibility Criteria

Inclusion Criteria

• Informed consent
• Subject has provided an appropriately signed and dated informed consent.
• Otherwise healthy outpatient with fall allergy
• Subject is treatable on an outpatient basis.
• Age
• 18 years or age or older at time of Visit 2
• Male or eligible female
• Female subjects should not be enrolled if they plan to become pregnant during the time of study participation. A urine pregnancy test will be required of all females at all visits to determine if the subject is pregnant.
• To be eligible for entry into the study, females of childbearing potential must commit to the consistent and correct use of an acceptable method of birth control, as defined by the following:
• Abstinence
• Females of childbearing potential who are not sexually active must commit to complete abstinence from intercourse for two weeks before exposure to the study drug, throughout the clinical trial, and for a period after the trial to account for elimination of the drug (minimum of six days).
• Oral contraceptive (either combined estrogen/progestin or progestin only)
• Injectable progestogen
• Implants of levonorgestrel
• Percutaneous contraceptive patches
• Intrauterine device (IUD) or intrauterine system (IUS) with a documented failure rate of less than 1% per year,
• Male partner who is sterile (vasectomy with documentation of azoospermia) prior to the female subject's entry into the study and is the sole sexual partner for that female subject
• Double barrier method-condom or occlusive cap (diaphragm or cervical /vault caps) plus spermicide
• Estrogenic vaginal ring
• Diagnosis of SAR
• SAR is defined as follows:
• A clinical history (written or verbal) of SAR with seasonal allergy symptoms (nasal symptoms) during each of the last two fall allergy seasons, and
• A positive skin test (by prick method) to fall allergen prevalent to the geographic area during the conduct of the study, within 12 months prior to Visit 1 or at Visit 1.
• A positive skin test is defined as a wheal 3 mm larger than the diluent control for prick testing.
• In vitro tests for specific IgE (such as RAST, PRIST) will not be allowed as a diagnosis of SAR.
• Subjects who meet the above criteria and who may also have perennial allergic rhinitis or vasomotor rhinitis are eligible for randomization.
• Adequate exposure to seasonal pollen
• Subject resides within a geographical region where exposure to fall seasonal allergen is expected to be significant during the entire study period.
• Subject does not plan to travel outside this area for more than 48 hours of the study period.
• Ability to comply with study procedures
• Subject understands and is willing, able and likely to comply with study procedures and restrictions.
• Literate
• Subject must be able to read, comprehend, and record information in English.

Exclusion Criteria

• Recent use (less than 1 year) of using branded (FLONASE) or generic FPNS or use of FFNS (VERAMYST).
• Significant concomitant medical conditions, defined as but not limited to:
• A historical or current evidence of clinically significant uncontrolled disease of any body system (e.g., tuberculosis, psychological disorders, eczema). Significant is defined as any disease that, in the opinion of the investigator, would put the safety of the subject at risk through study participation or which would confound the interpretation of the study results if the disease/condition exacerbated during the study.
• A severe physical obstruction of the nose (e.g., deviated septum or nasal polyp) or nasal septal perforation that could affect the deposition of intranasal study drug
• Nasal (eg, nasal septum) injury or surgery in the last 3 months
• Asthma, with the exception of mild intermittent asthma [National Asthma Education and Prevention Program (NARPP) Guidelines, 2002].
• Rhinitis medicamentosa
• Bacterial or viral infection (e.g., common cold) of the eyes or upper respiratory tract within two weeks of Visit 1 or during the screening period
• Documented evidence of acute or significant chronic sinusitis, as determined by the individual investigator
• Current or history of glaucoma and/or cataracts or ocular herpes simplex Physical impairment that would affect subject's ability to participate safely and fully in the study
• Clinical evidence of a Candida infection of the nose
• History of psychiatric disease, intellectual deficiency, poor motivation, substance abuse (including drug and alcohol) or other conditions that will limit the validity of informed consent or that would confound the interpretation of the study results
• History of adrenal insufficiency
• History of shingles
• Chickenpox or measles: A subject is not eligible if he/she currently has chickenpox or measles, or has been exposed to chickenpox or measles during the last 3 weeks and is non-immune. If a subject develops chickenpox or measles during the study, he/she will be withdrawn from the study. If a non-immune subject is exposed to chickenpox or measles during the study, his/her continuation in the study will be at the discretion of the investigator, taking into consideration the likelihood of developing active disease.
• Use of other corticosteroids, defined as:
• Intranasal corticosteroid within four weeks prior to Visit 1.
• Inhaled, oral, intramuscular, intravenous, ocular, and/or dermatological corticosteroid (with the exception of hydrocortisone cream/ointment, 1% or less) within eight weeks prior to Visit 1.
• Use of other allergy medications within the timeframe indicated relative to Visit 1
• Intranasal cromolyn within 14 days prior to Visit 1
• Short-acting prescription and OTC antihistamines, including antihistamines contained in insomnia and 'nighttime' pain formulations taken for insomnia, within 3 days prior to Visit 1
• Long-acting antihistamines within 10 days prior to Visit 1: loratadine, desloratadine, fexofenadine, cetirizine
• Oral or intranasal decongestants within 3 days prior to Visit 1
• Intranasal, oral, or inhaled anticholinergics within 3 days prior to Visit 1
• Oral antileukotrienes within 3 days prior to Visit 1
• Subcutaneous omalizumab (Xolair) within 5 months of Visit 1
• Intranasal antihistamines (e.g. Astelin) within 2 weeks prior to Visit 1
• Use of other medications that may affect allergic rhinitis or its symptoms
• Chronic use of concomitant medications, such as tricyclic antidepressants, that would affect assessment of the effectiveness of the study drug
• Chronic use of long-acting beta-agonists (e.g., salmeterol)
• Chronic use of other intranasally administered medications (e.g., calcitonin-salmon)
• Nasal irrigation solutions
• Use of immunosuppressive medications 8 weeks prior to screening and during the study
• Use of any medications that significantly inhibit the cytochrome P450 subfamily enzyme CYP3A4, including ritonavir and ketoconazole
• Immunotherapy
• Subjects may be enrolled into the study if the immunotherapy was not initiated within 30 days of Visit 1, if the dose has remained fixed over the 30 days prior to Visit 1, and the dose will remain fixed for the duration of the study.
• Allergy/Intolerance
• Known hypersensitivity to corticosteroids or any excipients in the product
• Clinical trial/experimental medication experience
• Has recent exposure to an investigational study drug within 30 days of Visit 1
• Participation in a previous or current GSK FFNS study
• Positive or inconclusive pregnancy test or female who is breastfeeding
• Has a positive or inconclusive pregnancy test at Visit 1 or Visit 2
• Affiliation with investigational site
• Subject is a participating investigator, sub-investigator, study co-ordinator, or employee of a participating investigator, or is an immediate family member of the aforementioned.
• Current tobacco use
• Subject currently uses smoking products including cigarettes, cigars, and pipe or chewing tobacco.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

GlaxoSmithKline

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

GSK Clinical Trials

Role: STUDY_DIRECTOR

GlaxoSmithKline

Locations

GSK Investigational Site

Birmingham, Alabama, United States

GSK Investigational Site

Phoenix, Arizona, United States

GSK Investigational Site

Long Beach, California, United States

GSK Investigational Site

Los Angeles, California, United States

GSK Investigational Site

San Diego, California, United States

GSK Investigational Site

San Diego, California, United States

GSK Investigational Site

San Francisco, California, United States

GSK Investigational Site

San Jose, California, United States

GSK Investigational Site

Vista, California, United States

GSK Investigational Site

Tallahassee, Florida, United States

GSK Investigational Site

Lilburn, Georgia, United States

GSK Investigational Site

Bangor, Maine, United States

GSK Investigational Site

Bethesda, Maryland, United States

GSK Investigational Site

Ocean City, New Jersey, United States

GSK Investigational Site

Ithaca, New York, United States

GSK Investigational Site

Rockville Centre, New York, United States

GSK Investigational Site

Collegeville, Pennsylvania, United States

GSK Investigational Site

Philadelphia, Pennsylvania, United States

GSK Investigational Site

Philadelphia, Pennsylvania, United States

GSK Investigational Site

Charleston, South Carolina, United States

GSK Investigational Site

Austin, Texas, United States

GSK Investigational Site

Austin, Texas, United States

GSK Investigational Site

Dallas, Texas, United States

GSK Investigational Site

Dallas, Texas, United States

GSK Investigational Site

Dallas, Texas, United States

GSK Investigational Site

El Paso, Texas, United States

GSK Investigational Site

New Braunfels, Texas, United States

GSK Investigational Site

San Antonio, Texas, United States

Countries

United States

References

Meltzer EO, Andrews C, Journeay GE, Lim J, Prillaman BA, Garris C, Philpot E. Comparison of patient preference for sensory attributes of fluticasone furoate or fluticasone propionate in adults with seasonal allergic rhinitis: a randomized, placebo-controlled, double-blind study. Ann Allergy Asthma Immunol. 2010 Apr;104(4):331-8. doi: 10.1016/j.anai.2010.02.010.

Reference Type: BACKGROUND

PMID: 20408344 (View on PubMed)

Study Documents

Document Type: Informed Consent Form

View Document

Document Type: Dataset Specification

View Document

Document Type: Clinical Study Report

View Document

Document Type: Annotated Case Report Form

View Document

Document Type: Individual Participant Data Set

View Document

Document Type: Statistical Analysis Plan

View Document

Document Type: Study Protocol

View Document

Related Links

https://www.clinicalstudydatarequest.com

Researchers can use this site to request access to anonymised patient level data and/or supporting documents from clinical studies to conduct further research.

Other Identifiers

FFU105927

Identifier Type: -

Identifier Source: org_study_id